Genetic disorders in children are mild to severe health problems, which occur when a gene (or genes) fails to express itself properly. This may result from a change in the gene, shifting of a gene ...

Genetics is the branch of science concerned with genes, heredity, and variation in living organisms. It seeks to understand the process of trait inheritance from parents to offspring, including ...

University of Otago – Ōtākou Whakaihu Waka has led international research uncovering a new genetic cause for a rare ...

Currently, 80 percent of early pregnancy losses aren't connected with a cause; most existing research examined the mare's ...

The Latham community will come together to celebrate the Tenth Annual Walk for Strength, a family-friendly event to raise ...

John Junior, a mental health campaigner from Manchester, said they felt misunderstood and 'different' throughout their ...

Myriad Genetics, Inc., a molecular diagnostic testing ... conducted using maternal blood to screen for severe chromosomal disorders in a fetus; Foresight Carrier Screen, a prenatal test for ...

In a groundbreaking study, researchers have linked rare “de novo” genetic mutations—copy number variants (CNVs)—to pediatric obsessive-compulsive disorder (OCD).

Journal of Medical Genetics (JMG) is a leading international peer-reviewed journal covering original research in human genetics, including reviews of and opinion on the latest developments. Articles ...

The conference represents a unique collaboration between the Prader-Willi Syndrome Association | USA (PWSA | USA), the Foundation for Prader-Willi Research (FPWR), and the International Prader-Willi ...

Down Syndrome, caused by an extra copy of chromosome 21, is one of the most common chromosomal disorders, marked by ...

Genomic DNA was isolated from bone marrow and/or peripheral blood samples of leukemia patients and sent to the DCAL (Frankfurt/Main, Germany). Patient samples were obtained from different study ...